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Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathy
Authors:Kumar N  Gross J B
Affiliation:N Kumar, Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA;J B Gross, Jr, Department of Medicine, Division of Gastroenterology and Hepatology, Mayo Clinic
Abstract:
Keywords:copper   myelopathy   ATP7A
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